홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

(3,4-Dihydro-2H-1-thia-4a,9-diaza-fluoren-6-yl)-methanol → Benzo[4,5]imidazo[2,1-b]thiazole-6-carbaldehyde

HRID 638899
노트
인쇄 미리보기

반응식

HRID 638899 반응식
[S:1]1[C:13]2[N:5]([C:6]3[C:11]([N:12]=2)=[CH:10][CH:9]=[C:8]([CH2:14][OH:15])[CH:7]=3)[CH2:4][CH2:3]C1>[O-2].[O-2].[Mn+4].C(Cl)(Cl)Cl>[S:1]1[CH:3]=[CH:4][N:5]2[C:6]3[CH:7]=[C:8]([CH:14]=[O:15])[CH:9]=[CH:10][C:11]=3[N:12]=[C:13]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 22224508(3,4-Dihydro-2H-1-thia-4a,9-diaza-fluoren-6-yl)-methanol

생성물 1

HCID 22224493Benzo[4,5]imidazo[2,1-b]thiazole-6-carbaldehyde

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6212Chloroform용매

실험 절차

To a round bottomed flask was loaded 1.16 grams of (3,4-Dihydro-2H-1-thia-4a,9-diaza-fluoren-6-yl)-methanol, 25 grams of manganese dioxide and 250 ml chloroform. The mixture was stirred for one hour at room temperature and then filtered through a pad of celite. This yielded 0.42 grams of product (42%). MS: 203.0 (M+H). H-NMR (CDCl3): δ 10.10 (ss, 1H), 8.24 (ss, 1H), 7.85 (m, 3H), 6.96 (m, 1H).

후처리

  1. customTo a round bottomed flask was loaded
  2. filtrationfiltered through a pad of celite

출처 및 근거

ORD 기록
ord-5a22d186a0504eb9ad3317e7eeacfe8a
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691842B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트